S. Leblond

1.8k citations

11 papers · 1.5k indexed · 1 hit paper · h-index 7

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments

Papers in

Cellular and Molecular Neuroscience 7
- Genetic Neurodegenerative Diseases 7
Physiology 1

Co-authors: Robert G. Korneluk Bé Wieringa Gary Shutler Catherine Tsilfidis Mani S. Mahadevan Kim O'Hoy Chris T. Amemiya Pieter J. de Jong
Journals: Nucleic Acids Research (4 papers)Genomics (2 papers)Human Genetics (1 paper)Science (1 paper)Human Heredity (1 paper)
Partner nations: Canada United States Netherlands

In The Last Decade

S. Leblond

11 papers receiving 1.4k citations

Hit Papers

align trajectories log scale

Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene 1992 · 1.3k citations

Peers

Countries citing papers authored by S. Leblond

Since Specialization

Citations

This map shows the geographic impact of S. Leblond's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by S. Leblond with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Leblond more than expected).

Fields of papers citing papers by S. Leblond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Leblond. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by S. Leblond. The network helps show where S. Leblond may publish in the future.

Co-authorship network

The 25 scholars most cited alongside S. Leblond, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with S. Leblond Line = papers co-authored together S. Leblond links everyone, so they are left out of the graph.

All Works

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11 of 11 papers shown

#	Work
1	Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene Science ·Mani S. Mahadevan, Catherine Tsilfidis, Luc A. Sabourin, Gary Shutler, Chris T. Amemiya, Gert Jansen, Catherine Neville, Monica Narang, Juana Barceló, Kim O'Hoy, S. Leblond, O. V. Peneva, Pieter J. de Jong, Bé Wieringa, Robert G. Korneluk Hit paper breakdown →	1992	1340
2	DNA Polymorphism and Linkage Disequilibrium within the Apolipoprotein CII Locus on Human Chromosome 19 Human Heredity ·Alex MacKenzie, Agnieszka Olechnicka, S. Leblond, AR Korabik, Guilherme de Castro Rezende, Robert G. Korneluk	1991	2
3	Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms Human Genetics ·J Bailly, Lomgen PHOUNGMALAYP, S. Leblond, Regiane Ferrari de Castro	1991	11
4	An Sstl RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3 Nucleic Acids Research ·Catherine Tsilfidis, Gary Shutler, S. Leblond, Robert G. Korneluk	1991	4
5	RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3 Nucleic Acids Research ·Gary Shutler, Catherine Tsilfidis, S. Leblond, Robert G. Korneluk	1991	4
6	An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3 Nucleic Acids Research ·Gary Shutler, S. Leblond, J Bailly, Alex MacKenzie, Catherine Tsilfidis, Robert G. Korneluk	1991	4
7	Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy Genomics ·Gary Shutler, Alex MacKenzie, Han G. Brunner, Bé Wieringa, Peter J. de Jong, Frans P. Lohman, S. Leblond, J Bailly, Robert G. Korneluk	1991	15
8	D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q. PubMed ·Catherine Tsilfidis, A.E. MacKenzie, Gary Shutler, S. Leblond, J Bailly, Keith Johnson, R. Williamson, J. Siegel‐Bartelt, Robert G. Korneluk, Peggy Shelbourne	1991	12
9	Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): Application to myotonic dystrophy diagnosis Genomics ·Christian Lavedan, C Duros, D. Savoy, S. Leblond, J Bailly, Robert G. Korneluk, Claudine Junien	1990	8
10	The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy. PubMed ·Noemi Piredda, Robert G. Korneluk, Francesco Zorzato, Junichi Fujii, Michael J. Phillips, David Iles, Bé Wieringa, S. Leblond, J Bailly, H.F. Willard	1990	61
11	Avall RFLP at the human apolipoprotein CII (APO CII) gene locus Nucleic Acids Research ·Robert G. Korneluk, Agnieszka Olechnicka, S. Leblond, AR Korabik, Francisco E. Baralle, Alasdair G. W. Hunter	1987	10

About S. Leblond

S. Leblond is a scholar working on Cellular and Molecular Neuroscience, Physiology, Immunology and Allergy, Molecular Biology and Ophthalmology, having authored 11 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), RNA modifications and cancer (3 papers), DNA and Nucleic Acid Chemistry (2 papers), DNA Repair Mechanisms (2 papers), Mitochondrial Function and Pathology (2 papers), Biochemical and Molecular Research (2 papers), Cardiomyopathy and Myosin Studies (2 papers) and Ion channel regulation and function (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (1.2k citations), Neurology (386 citations), Molecular Biology (1.3k citations), Cardiology and Cardiovascular Medicine (212 citations) and Genetics (218 citations). S. Leblond has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include Robert G. Korneluk, Bé Wieringa, Gary Shutler, Catherine Tsilfidis, Mani S. Mahadevan, Kim O'Hoy, Chris T. Amemiya, Pieter J. de Jong, Gert Jansen and Juana Barceló. Their work appears in journals such as Nucleic Acids Research, Genomics, Human Genetics, Science and Human Heredity.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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